Insulin isophane biphasic porcine 30/70 100units/ml suspension for injection 1.5ml cartridges
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Hypurin Porcine 30/70 Mix 100units/ml suspension for injection 1.5ml cartridges
WHO defined daily dose (DDD)
40 unit
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 5 · Randomised trials: 4 · 1980–2026
Showing the 50 most relevant studies, sorted by most relevant.
Hemmingsen B, Metzendorf MI, Richter B
2021
- Myocardial Infarction
- Diabetes Mellitus, Type 1
- Hypoglycemia
G. M. Cruise, O. Hegre, F. Lamberti, et al.
Cell Transplantation, 1999
J.J. Holst, C. Ørskov, O. Vagn Nielsen, et al.
FEBS Letters, 1987
Raymond Y.N. Lee, Jürgen Hench, Gary Ruvkun
Current Biology, 2001
M ESLER
American Journal of Hypertension, 2001
F.J Carter, T.G Frank, P.J Davies, et al.
Medical Image Analysis, 2001
Waugh Norman, Christine Clar, Clar Christine, et al.
Public Library of Science, 2009
Julia Steinberger, Antoinette Moran, Ching-Ping Hong, et al.
The Journal of Pediatrics, 2001
John E. Nestler, Dale Stovall, Nausheen Akhter, et al.
Fertility and Sterility, 2002
Manfred Hecking, Marcus D. Säemann (606867), Marlies Antlanger (3615428), et al.
Public Library of Science (PLoS), 2018
Treating hyperglycemia in previously non-diabetic individuals with exogenous insulin immediately after kidney transplantation reduced the odds of developing Posttransplantation Diabetes Mellitus (PTDM) in our previous proof-of-concept clinical trial. We hypothesized that insulin-pump therapy with maximal insulin dosage during the afternoon would improve glycemic control compared to basal insulin and standard-of-care. In a multi-center, randomized, controlled trial testing insulin isophane for PTDM prevention, we added a third study arm applying continuous subcutaneous insulin lispro infusion (CSII) treatment. CSII was initiated in 24 patients aged 55±12 years, without diabetes history, receiving tacrolimus. The mean daily insulin lispro dose was 9.2±5.2 IU. 2.3±1.1% of the total insulin dose were administered between 00:00 and 6:00, 19.5±11.6% between 6:00 and 12:00, 62.3±15.6% between 12:00 and 18:00 and 15.9±9.1% between 18:00 and 24:00. Additional bolus injections were necessary in five patients. Mild hypoglycemia (52–60 mg/dL) occurred in two patients. During the first post-operative week glucose control in CSII patients was overall superior compared to standard-of-care as well as once-daily insulin isophane for fasting and post-supper glucose. We present an algorithm for CSII treatment in kidney transplant recipients, demonstrating similar safety and superior short-term efficacy compared to standard-of-care and once-daily insulin isophane.</div
Abstract licence: CC BY
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.